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Release and Constancy of an Antibiotic Resistance Gene in Seawater Under Grazing Stress by Ciliates and Heterotrophic Nanoflagellates

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Date 2017 Jun 9
PMID 28592722
Citations 7
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Abstract

Extracellular DNA (exDNA) is released from bacterial cells through various processes. The antibiotic resistance genes (ARGs) coded on exDNA may be horizontally transferred among bacterial communities by natural transformation. We quantitated the released/leaked tetracycline resistance gene, tet(M) over time under grazing stress by ciliates and heterotrophic nanoflagellates (HNFs), and found that extracellular tet(M) (ex-tetM) increased with bacterial grazing. Separate microcosms containing tet(M)-possessing bacteria with ciliates or HNFs were prepared. The copy number of ex-tetM in seawater in the ciliate microcosm rapidly increased until 3 d after the incubation, whereas that in the HNF microcosm showed a slower increase until 20 d. The copy number of ex-tetM was stable in both cases throughout the incubation period, suggesting that extracellular ARGs are preserved in the environment, even in the presence of grazers. Additionally, ARGs in bacterial cells were constant in the presence of grazers. These results suggest that ARGs are not rapidly extinguished in a marine environment under grazing stress.

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References
1.
Kobayashi T, Suehiro F, Tuyen B, Suzuki S . Distribution and diversity of tetracycline resistance genes encoding ribosomal protection proteins in Mekong river sediments in Vietnam. FEMS Microbiol Ecol. 2007; 59(3):729-37. DOI: 10.1111/j.1574-6941.2006.00244.x. View

2.
Davison P . THE EFFECT OF HYDRODYNAMIC SHEAR ON THE DEOXYRIBONUCLEIC ACID FROM T(2) AND T(4) BACTERIOPHAGES. Proc Natl Acad Sci U S A. 1959; 45(11):1560-8. PMC: 222760. DOI: 10.1073/pnas.45.11.1560. View

3.
Torti A, Lever M, Jorgensen B . Origin, dynamics, and implications of extracellular DNA pools in marine sediments. Mar Genomics. 2015; 24 Pt 3:185-96. DOI: 10.1016/j.margen.2015.08.007. View

4.
Ochman H, Lawrence J, Groisman E . Lateral gene transfer and the nature of bacterial innovation. Nature. 2000; 405(6784):299-304. DOI: 10.1038/35012500. View

5.
Nielsen K, Johnsen P, Bensasson D, Daffonchio D . Release and persistence of extracellular DNA in the environment. Environ Biosafety Res. 2007; 6(1-2):37-53. DOI: 10.1051/ebr:2007031. View